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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 2020

FusionGeneSummary for AP1B1_NIPSNAP1

check button Fusion gene summary
Fusion gene informationFusion gene name: AP1B1_NIPSNAP1
Fusion gene ID: 2020
HgeneTgene
Gene symbol

AP1B1

NIPSNAP1

Gene ID

162

8508

Gene nameadaptor related protein complex 1 subunit beta 1nipsnap homolog 1
SynonymsADTB1|AP105A|BAM22|CLAPB2-
Cytomap

22q12.2

22q12.2

Type of geneprotein-codingprotein-coding
DescriptionAP-1 complex subunit beta-1ADTB1, CLAPB2Golgi adaptor HA1/AP1 adaptin beta subunitadapter-related protein complex 1 subunit beta-1adaptor protein complex AP-1 subunit beta-1adaptor related protein complex 1 beta 1 subunitbeta-1-adaptinbeta-adaptin protein NipSnap homolog 14-nitrophenylphosphatase domain and non-neuronal SNAP25-like 1
Modification date2018052220180523
UniProtAcc

Q10567

Q9BPW8

Ensembl transtripts involved in fusion geneENST00000356015, ENST00000432560, 
ENST00000357586, ENST00000405198, 
ENST00000317368, ENST00000402502, 
ENST00000415447, ENST00000472057, 
ENST00000216121, ENST00000494966, 
Fusion gene scores* DoF score7 X 7 X 5=2456 X 3 X 6=108
# samples 76
** MAII scorelog2(7/245*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: AP1B1 [Title/Abstract] AND NIPSNAP1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID

check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVBLCATCGA-FD-A5BT-01AAP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000356015ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
5CDS-intronENST00000356015ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
Frame-shiftENST00000432560ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
5CDS-intronENST00000432560ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
Frame-shiftENST00000357586ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
5CDS-intronENST00000357586ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
Frame-shiftENST00000405198ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
5CDS-intronENST00000405198ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
Frame-shiftENST00000317368ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
5CDS-intronENST00000317368ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
Frame-shiftENST00000402502ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
5CDS-intronENST00000402502ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
Frame-shiftENST00000415447ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
5CDS-intronENST00000415447ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
intron-3CDSENST00000472057ENST00000216121AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-
intron-intronENST00000472057ENST00000494966AP1B1chr22

29745207

-NIPSNAP1chr22

29954942

-

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FusionProtFeatures for AP1B1_NIPSNAP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
AP1B1

Q10567

NIPSNAP1

Q9BPW8

Subunit of clathrin-associated adaptor protein complex 1that plays a role in protein sorting in the late-Golgi/trans-Golginetwork (TGN) and/or endosomes. The AP complexes mediate both therecruitment of clathrin to membranes and the recognition ofsorting signals within the cytosolic tails of transmembrane cargomolecules.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

.

* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for AP1B1_NIPSNAP1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for AP1B1_NIPSNAP1


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors
AP1B1AP1G1, PRKDC, ATM, ATR, ARF1, CLINT1, AMPH, CLTC, CABIN1, KIF13A, AP2M1, AP1M1, SNCA, SIRT7, CUL3, CDK2, COPS5, SHBG, EPN1, EPS15, SNAP91, AP1S2, AP1S1, BARD1, VCP, NTRK2, PPP6R3, ABCE1, DIABLO, INTS9, TBC1D2, TRIP10, TRMT61A, RPA3, RPA2, RPA1, EGFR, CCDC183, NECAP2, LRFN4, PNKD, AP1M2, CCNL2, AP2A1, AP2A2, CBS, ARHGAP1, FLNB, PRKAB1, TTC37, UBA1, NTRK1, ARRB2, TMEM17, XPO1, GTSE1, SNW1, CDC5L, AP2S1, ARFGAP1, RUNDC3A, GPR156, SNX9, PPP6R2, LSR, GPBP1L1, FBXO4, FCHO1, STAMBPL1, HIP1R, SIGLECL1, SHC1, MTUS2, MTNR1B, DLD, TRIM25, SLC2A8NIPSNAP1RGS2, GABARAPL1, GABARAPL2, GBAS, MAP1LC3A, MAP1LC3B, SQSTM1, ICT1, PRKCI, DBI, CDH1, NPM1, AMOT, CTTNBP2NL, PARK2, VCP, ENO1, SHMT2, MOV10, NXF1, CUL7, OBSL1, FOXRED2, UBE2A, UBE2B, KCMF1, NTRK1, TCTN3, XPO1, CCT6A, FAT1, HSPD1, PLEC, PRKAA2, TCF20, TCP1, CCT3, BCL7B, GTF3C5, KNTC1, CCT7, CCT4, CCT2, IVNS1ABP, CCT8, HPSE, POP1, FNDC3A, CCT5, GANAB, ARHGEF12, ZNF281, C10orf12, HP1BP3, HAUS6, MRPS18A, ASCC2, TNRC18, DNAJC21, NSMCE2, GABARAP, COQ9, NDUFA4, CISD3, NDUFS3, C15orf48, CHCHD2, PTPMT1, IFT140, WDR19


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for AP1B1_NIPSNAP1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for AP1B1_NIPSNAP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource